US4754030A - Cefbuperazone crystalline triethylamine salt - Google Patents

Cefbuperazone crystalline triethylamine salt Download PDF

Info

Publication number
US4754030A
US4754030A US06/697,172 US69717285A US4754030A US 4754030 A US4754030 A US 4754030A US 69717285 A US69717285 A US 69717285A US 4754030 A US4754030 A US 4754030A
Authority
US
United States
Prior art keywords
cefbuperazone
crystalline
salt
triethylamine salt
triethylamine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
US06/697,172
Other languages
English (en)
Inventor
Murray A. Kaplan
Robert A. Lipper
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bristol Myers Co
Original Assignee
Bristol Myers Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bristol Myers Co filed Critical Bristol Myers Co
Priority to US06/697,172 priority Critical patent/US4754030A/en
Assigned to BRISTOL-MYERS COMPANY reassignment BRISTOL-MYERS COMPANY ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: KAPLAN, MURRAY A., LIPPER, ROBERT A.
Priority to CA000499856A priority patent/CA1242700A/en
Priority to DE8686101309T priority patent/DE3687171T2/de
Priority to EP86101309A priority patent/EP0189942B1/de
Priority to AT86101309T priority patent/ATE82978T1/de
Priority to JP61020000A priority patent/JPH0631257B2/ja
Application granted granted Critical
Publication of US4754030A publication Critical patent/US4754030A/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/57—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with a further substituent in position 7, e.g. cephamycines

Definitions

  • the present invention refers to the stable crystalline triethylamine salt of cefbuperazone, a cephalosporin antibiotic (Class 424, Subclass 246).
  • Cefbuperazone is a so-called second generation injectable cephalosporin which has the following structure and is the subject of U.S. Pat. No. 4,263,292 patented Apr. 21, 1981. ##STR1##
  • the sodium salt of cefbuperazone is under clinical development in Japan by Toyama Chemical Co., Ltd.
  • the following table contains stability data from tests conducted on the particular salt forms of cefbuperazone indicated in the table.
  • the crystalline-TEA (triethylamine) salt was prepared as described below.
  • the amorphous-Na were prepared by a lyophilization process substantially as disclosed in U.S. Pat. No. 4,263,292.
  • the amorphous-TEA salt was prepared by lyophilization of an aqueous solution thereof have pH 6.0, and prepared from the antibiotic and 1.1 molar proportions of triethylamine.
  • the crystalline triethylamine salt exhibits highly satisfactory stability characteristics when stored in the dry state. No loss was observed when stored for 4 months at 37° C. At 45° C. the loss in activity during 2 weeks storage for the crystalline triethylamine salt was 2.8% as compared to 12% for the amorphous triethylamine salt and 27% for the amorphous sodium salt. During a total of 8 weeks storage at this temperature, the crystalline-TEA salt suffered no further loss. Similarly at 56° C.
  • the crystalline salt of the present invention has been characterized by elemental analysis, melting point determined with a differential scanning calorimeter, X-ray powder diffraction pattern, and infra-red spectrum. In the nuclear magnetic resonance spectrum, chemical shifts, characteristic of the cefbuperazone CH 3 protons are obscured by the triethylamine. The data with respect thereto appear herein.
  • a critical feature in the preparation of the crystalline triethylamine salt of the present invention is the use of methylene chloride or of methylene chloride containing up to 10% by volume of a CH 2 Cl 2 -miscible water soluble oxygenated organic solvent as the reaction medium.
  • Suitable oxygenated organic solvents include ethyl acetate, acetone, tetrahydrofuran, and a lower alkanol such as ethanol, isopropanol, or butanol.
  • Methanol may be employed, but this solvent has an inclination to rupture the beta-lactam ring by a solvolytic process and it is desirable to avoid contact with methanol.
  • the salt forms on contact of the ingredients at room temperature, 20°-25° C.
  • reaction solution may be employed for sterilization and purification purposes and if aseptic technique is used for the crystallization step using the oxygenated organic solvent, material suitable for parenteral formulations may be produced. This is illustrated in the following procedure.
  • cefbuperazone used as starting material in the foregoing procedure is not critical.
  • the dihydrate described in U.S. Pat. No. 4,263,292 is quite satisfactory, but dehydrated material may be used without any advantage.
  • the infra-red absorption spectrum prepared using a pelletized KBr dilution of the crystalline material is illustrated in FIG. 1 hereof.
  • the NMR spectrum is as follows: ⁇ , ppm (D 2 O, TSP as reference): 5.16 (singlet, integral 1); 4.08 (singlet, integral 3); 3.58 (singlet, integral 3); 4.2-4.4 (quartet, J ca 7 Hz), integral 6); and 1.0-1.5 (overlap patterns, integral 15).
  • the X-ray powder diffraction pattern was determined on a Rigaku X-Ray Powder Diffractometer using a Cu 25 kv lamp operated at 20 ma, at a scan rate of 2° per minute from 40° to 5° using a chart speed of 10 mm per minute and a nickel filter.
  • the d-spacings calculated from these measurements are listed below.
  • the relative intensities were estimated by measurement of the peak heights on a tracing corresponding to the d-spacings.
  • the crystalline cefbuperazone-TEA salt of this invention is soluble in water in a wide range of proportions. It readily dissolves in the common injection vehicles including water, 5% glucose, and saline. It is substantially insoluble in the common organic solvents except methylene chloride and similar halogenated lower alkanes.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Cephalosporin Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
US06/697,172 1985-02-01 1985-02-01 Cefbuperazone crystalline triethylamine salt Expired - Fee Related US4754030A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
US06/697,172 US4754030A (en) 1985-02-01 1985-02-01 Cefbuperazone crystalline triethylamine salt
CA000499856A CA1242700A (en) 1985-02-01 1986-01-20 Cefbuperazone crystalline triethylamine salt
DE8686101309T DE3687171T2 (de) 1985-02-01 1986-01-31 Kristallines triethylaminsalz von cefbuperazon.
EP86101309A EP0189942B1 (de) 1985-02-01 1986-01-31 Kristallines Triethylaminsalz von Cefbuperazon
AT86101309T ATE82978T1 (de) 1985-02-01 1986-01-31 Kristallines triethylaminsalz von cefbuperazon.
JP61020000A JPH0631257B2 (ja) 1985-02-01 1986-01-31 セフブペラゾンの結晶性トリエチルアミン塩

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US06/697,172 US4754030A (en) 1985-02-01 1985-02-01 Cefbuperazone crystalline triethylamine salt

Publications (1)

Publication Number Publication Date
US4754030A true US4754030A (en) 1988-06-28

Family

ID=24800099

Family Applications (1)

Application Number Title Priority Date Filing Date
US06/697,172 Expired - Fee Related US4754030A (en) 1985-02-01 1985-02-01 Cefbuperazone crystalline triethylamine salt

Country Status (6)

Country Link
US (1) US4754030A (de)
EP (1) EP0189942B1 (de)
JP (1) JPH0631257B2 (de)
AT (1) ATE82978T1 (de)
CA (1) CA1242700A (de)
DE (1) DE3687171T2 (de)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5496345A (en) * 1992-06-02 1996-03-05 General Surgical Innovations, Inc. Expansible tunneling apparatus for creating an anatomic working space
US6592602B1 (en) 1999-10-08 2003-07-15 General Surgical Innovations, Inc. Balloon dissection apparatus
US6632234B2 (en) 1992-06-02 2003-10-14 General Surgical Innovations, Inc. Apparatus and method for developing an anatomic space for laparoscopic procedures with laparoscopic visualization
US6835829B2 (en) 1995-08-14 2004-12-28 Sandoz Gmbh Purification process
US20100147428A1 (en) * 2006-12-15 2010-06-17 Lipper Ray W Wheel having inner bead-lock
WO2022235105A1 (ko) * 2021-05-06 2022-11-10 주식회사 엘지화학 멜라노코르틴 수용체 작용제 화합물의 결정형 ⅶ 및 이의 제조방법

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101830916B (zh) * 2010-05-14 2013-08-14 胡梨芳 抗菌药物及其制备方法和用途
CN102327240B (zh) * 2011-09-30 2013-03-27 海南合瑞制药股份有限公司 一种注射用头孢拉宗钠药物组合物及其制备方法
CN113069422B (zh) * 2021-04-20 2022-07-12 海南通用三洋药业有限公司 注射用头孢拉宗钠冻干粉针剂的制备方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1104938A (en) * 1964-05-28 1968-03-06 Glaxo Lab Ltd Improvements in or relating to 7-aminocephalosporanic acid
US4160863A (en) * 1977-04-07 1979-07-10 Bristol-Myers Company Process for the preparation of the crystalline monohydrate of 7-[D-α-aα-(p-hydroxyphenyl)acetamido]-3-methyl-3-cephem-4-carboxylic acid
US4263292A (en) * 1978-06-13 1981-04-21 Toyama Chemical Co., Ltd. 7α-methoxycephalosporins and pharmaceutical composition comprising the same

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5625188A (en) * 1979-08-07 1981-03-10 Toyama Chem Co Ltd 7alpha-methoxycephalosporin
GB8316589D0 (en) * 1983-06-17 1983-07-20 Ici Plc Crystalline salts

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1104938A (en) * 1964-05-28 1968-03-06 Glaxo Lab Ltd Improvements in or relating to 7-aminocephalosporanic acid
US4160863A (en) * 1977-04-07 1979-07-10 Bristol-Myers Company Process for the preparation of the crystalline monohydrate of 7-[D-α-aα-(p-hydroxyphenyl)acetamido]-3-methyl-3-cephem-4-carboxylic acid
US4263292A (en) * 1978-06-13 1981-04-21 Toyama Chemical Co., Ltd. 7α-methoxycephalosporins and pharmaceutical composition comprising the same

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060036277A1 (en) * 1992-06-02 2006-02-16 Kieturakis Maciej J Apparatus and method for developing an anatomic space for laparoscopic hernia repair and patch for use therewith
US6695856B2 (en) 1992-06-02 2004-02-24 General Surgical Innovations, Inc. Apparatus and methods for developing an anatomic space for laparoscopic hernia repair and patch for use therewith
US8187296B2 (en) 1992-06-02 2012-05-29 Tyco Healthcare Group Lp Apparatus and method for developing an anatomic space for laparoscopic hernia repair and patch for use therewith
US6632234B2 (en) 1992-06-02 2003-10-14 General Surgical Innovations, Inc. Apparatus and method for developing an anatomic space for laparoscopic procedures with laparoscopic visualization
US6679900B2 (en) 1992-06-02 2004-01-20 General Surgical Innovations, Inc. Apparatus and methods for developing an anatomic space for laparoscopic hernia repair and patch for use therewith
US20040015182A1 (en) * 1992-06-02 2004-01-22 Kieturakis Maciej J. Apparatus and method for developing an anatomic space for laparoscopic procedures with laparoscopic visualization
US6953467B2 (en) 1992-06-02 2005-10-11 General Surgical Innovations, Inc. Apparatus and method for developing an anatomic space for laparoscopic hernia repair and patch for use therewith
US6755845B2 (en) 1992-06-02 2004-06-29 General Surgical Innovations, Inc. Apparatus and method for developing an anatomic space for laparoscopic hernia repair and patch for use therewith
US6758853B2 (en) 1992-06-02 2004-07-06 General Surgical Innovations, Inc. Apparatus and methods for developing an anatomic space for laparoscopic hernia repair and patch for use therewith
US20040236363A1 (en) * 1992-06-02 2004-11-25 Kieturakis Maciej J. Apparatus and methods for developing an anatomic space for laparoscopic hernia repair and patch for use therewith
US6514272B1 (en) 1992-06-02 2003-02-04 General Surgical Innovations, Inc. Apparatus and method for developing an anatomic space for laparoscopic hernia repair and patch for use therewith
US8157831B2 (en) 1992-06-02 2012-04-17 Tyco Healthcare Group Lp Apparatus and method for developing an anatomic space for laparoscopic procedures with laparoscopic visualization
US7297153B2 (en) 1992-06-02 2007-11-20 General Surgical Innovations, Inc. Apparatus and method for developing an anatomic space for laparoscopic hernia repair and patch for use therewith
US7001405B2 (en) 1992-06-02 2006-02-21 General Surgical Innovations, Inc. Apparatus and method for developing an anatomic space for laparoscopic procedures with laparoscopic visualization
US20060173483A1 (en) * 1992-06-02 2006-08-03 Kieturakis Maciej J Apparatus and method for developing an anatomic space for laparoscopic procedures with laparoscopic visualization
US7214236B2 (en) 1992-06-02 2007-05-08 General Surgical Innovations, Inc. Apparatus and methods for developing an anatomic space for laparoscopic hernia repair and patch for use therewith
US5496345A (en) * 1992-06-02 1996-03-05 General Surgical Innovations, Inc. Expansible tunneling apparatus for creating an anatomic working space
US20080058853A1 (en) * 1992-06-02 2008-03-06 Gneral Surgical Innovactions, Inc. Apparatus and method for developing an anatomic space for laparoscopic hernia repair and patch for use therewith
US6835829B2 (en) 1995-08-14 2004-12-28 Sandoz Gmbh Purification process
US8172869B2 (en) 1999-10-08 2012-05-08 Tyco Healthcare Group Lp Balloon dissection apparatus
US6592602B1 (en) 1999-10-08 2003-07-15 General Surgical Innovations, Inc. Balloon dissection apparatus
US20100147428A1 (en) * 2006-12-15 2010-06-17 Lipper Ray W Wheel having inner bead-lock
WO2022235105A1 (ko) * 2021-05-06 2022-11-10 주식회사 엘지화학 멜라노코르틴 수용체 작용제 화합물의 결정형 ⅶ 및 이의 제조방법
CN117255786A (zh) * 2021-05-06 2023-12-19 株式会社Lg 化学 黑皮质素受体激动剂化合物的晶型vii及其制备方法

Also Published As

Publication number Publication date
EP0189942A2 (de) 1986-08-06
CA1242700A (en) 1988-10-04
EP0189942B1 (de) 1992-12-02
DE3687171D1 (de) 1993-01-14
DE3687171T2 (de) 1993-04-01
ATE82978T1 (de) 1992-12-15
JPH0631257B2 (ja) 1994-04-27
JPS61180789A (ja) 1986-08-13
EP0189942A3 (en) 1987-09-30

Similar Documents

Publication Publication Date Title
US6441162B2 (en) Crystalline substance of cefditoren pivoxyl and the production of the same
AU615509B2 (en) Temperature stable crystalline salts of 7-(alpha-(2- aminothiazol-4-yl)-alpha-(Z)-methoxyiminoacetamidol)-3- ((1-methyl-1-pyrrolidino)methyl)-3-cephem-4-carboxylate
US4754030A (en) Cefbuperazone crystalline triethylamine salt
EP0189941B1 (de) Antibiotika
AU597262B2 (en) Cephalosporin salts and injectable compositions
US4006138A (en) Crystalline form of sodium O-formylcefamandole
US4104470A (en) Crystallization process for cefazolin sodium
US4054738A (en) Sodium cefamandole crystalline forms
US5244891A (en) Injectable compositions of cefepime dihydrochloride hydrate
EP0587121B1 (de) Kristallisiertes Dihydrat eines Cephalosporin-Dihydrochlorids und seine injizierbaren Zusammensetzungen
US4680389A (en) Temperature stable crystalline di(1-methyl-2-pyrralidinone) and di(N-formylpyrrolidine) adducts of cephalosporin derivatives
US4994451A (en) Cephalosporin salts and injectable compositions
CA1282407C (en) Crystalline cephem carboxylic acid addition salt
US3947414A (en) Cefamandole derivatives
EP0039967B1 (de) Amoxicillinsolvat, Verfahren zur Herstellung und Verfahren zur Herstellung von dieses Solvat enthaltenden injizierbaren Präparaten
KR840000036B1 (ko) 옥사-β-락탐 2산 화합물의 D-세스퀴나트륨염의 제조방법
US3947415A (en) Cefamandole derivatives
US3708478A (en) A crystalline complex of cephaloridine with an alkane diol
US4048158A (en) d-α-Isobutylsulfobenzylpenicillin hemi-solvate crystals
SU860705A3 (ru) Способ получени кристаллической формы D-конфигурации диаммониевой соли 7 - -карбокси- -( -оксифенил)ацетамидо/-7 -метокси-3-(1-метилтетразол-5-ил)-тиометил-1-оксадетиа-3-цефем-4-карбоновой кислоты
KR0169534B1 (ko) 고밀도의 고결정성 세포페라존 나트륨염 및 그의 제조방법
US5401842A (en) Injectable compositions of a cephalosporin dihydrate salt
JP2653480B2 (ja) セフェム誘導体結晶
JPH01128985A (ja) 薬物動態学的に改良されたセファロスポリン誘導体、その製法、それを含む医薬組成物、及び成中間体

Legal Events

Date Code Title Description
AS Assignment

Owner name: BRISTOL-MYERS COMPANY 345 PARK AVE. NEW YORK, NY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNORS:KAPLAN, MURRAY A.;LIPPER, ROBERT A.;REEL/FRAME:004375/0797

Effective date: 19850128

FPAY Fee payment

Year of fee payment: 4

REMI Maintenance fee reminder mailed
LAPS Lapse for failure to pay maintenance fees
FP Lapsed due to failure to pay maintenance fee

Effective date: 19960703

STCH Information on status: patent discontinuation

Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362